The present invention is concerned with 2H-tetrazole-5-yl-amide derivatives ofgeneral formula (I) wherein R1 signifies hydrogen, lower alkyl, -(CH2)n-CF3, -(CH2)n-CHF2, -(CH2)n-CN, -(CH2)n-cycloalkyl, -(CH2)n-O-lower alkyl, -(CH2)n-O-cycloalkyl or -(CH2)n-C(O)O-lower alkyl; R2 signifies hydrogen, lower alkyl,lower alkoxy, halogen, -C(O)-lower alkyl, -C(O)OH, -C(O)O-lower alkyl, -NR3R4or -C(O)-NR3R4 and wherein R3 and R4 may be independently from each otherhydrogen or lower alkyl; X signifies -O-, -S-, -CH2, -OCH2- or two hydrogenatoms not forming a bridge; and n signifies 0, 1, 2, 3 or 4; as well as withtheir pharmaceutically acceptable salts. It has been found that the compoundsof general formula (I) are group 1 metabotropic glutamate receptor agonists(mGluR) and are therefore useful in the treatment of corresponding CNS-disorders.
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